van Haasteren G A, Linkels E, van Toor H, Klootwijk W, Kaptein E, de Jong F H, Reymond M J, Visser T J, de Greef W J
Department of Endocrinology and Reproduction, Erasmus University, Rotterdam, Netherlands.
J Endocrinol. 1996 Aug;150(2):169-78. doi: 10.1677/joe.0.1500169.
The reduced thyroid activity during short-term starvation is associated with a lowered hypothalamic synthesis and secretion of TRH. However, little is known about the cause of the reduced thyroid function during prolonged malnutrition. We have therefore studied the effects of food reduction to one-third of normal (FR33) on the hypothalamus-pituitary-thyroid axis of male and female Wistar rats. After 3 weeks body weights of FR33 rats were almost 50% lower than those of controls. In both sexes, FR33 caused marked increases in serum corticosterone, and decreases in serum TSH, thyroxine (T4), free T4, tri-iodothyronine (T3) and free T3. While the free T3 fraction (FFT3) in serum decreased, the free T4 fraction (FFT4) tended to increase. Electrophoretic analysis indicated that decreased FFT3 was correlated with an increased thyroxine-binding globulin, while the increase in FFT4 seemed due to a decreased thyroxine-binding prealbumin binding capacity. Total RNA and proTRH mRNA in the hypothalamus were not affected by FR33. Median eminence and posterior pituitary TRH content tended to increase in FR33 rats, suggesting that hypothalamic TRH release is reduced in FR33 rats. Anterior pituitary TSH content was decreased by FR33 in both sexes, but pituitary TSH beta mRNA and TRH receptor status were not affected except for increased pituitary TSH beta mRNA in female FR33 rats. Although FR33 had no effect on pituitary weight, pituitary RNA and membrane protein content in FR33 rats were 50-70% lower than values in controls. In conclusion, prolonged food reduction suppresses the pituitary-thyroid axis in rats. In contrast to short-term food deprivation, the mechanism whereby serum TSH is suppressed does not appear to involve decreases in proTRH gene expression, but may include effects on pituitary mRNA translation. Our results further support the hypothesis that TSH release may be lowered by increased corticosterone secretion, although the mechanism of this effect may differ between acute starvation and prolonged food reduction.
短期饥饿期间甲状腺活性降低与下丘脑促甲状腺激素释放激素(TRH)合成及分泌减少有关。然而,对于长期营养不良期间甲状腺功能降低的原因知之甚少。因此,我们研究了将食物摄入量减少至正常水平的三分之一(FR33)对雄性和雌性Wistar大鼠下丘脑 - 垂体 - 甲状腺轴的影响。3周后,FR33大鼠的体重比对照组低近50%。在两性中,FR33均导致血清皮质酮显著升高,血清促甲状腺激素(TSH)、甲状腺素(T4)、游离T4、三碘甲状腺原氨酸(T3)和游离T3降低。虽然血清中游离T3分数(FFT3)降低,但游离T4分数(FFT4)有升高趋势。电泳分析表明,FFT3降低与甲状腺素结合球蛋白增加相关,而FFT4升高似乎是由于甲状腺素结合前白蛋白结合能力降低。下丘脑的总RNA和proTRH mRNA不受FR33影响。FR33大鼠的正中隆起和垂体后叶TRH含量有增加趋势,提示FR33大鼠下丘脑TRH释放减少。FR33使两性垂体前叶TSH含量降低,但除雌性FR33大鼠垂体TSHβ mRNA增加外,垂体TSHβ mRNA和TRH受体状态不受影响。虽然FR33对垂体重量无影响,但FR33大鼠的垂体RNA和膜蛋白含量比对照组低50 - 70%。总之,长期食物减少会抑制大鼠的垂体 - 甲状腺轴。与短期食物剥夺不同,血清TSH受抑制的机制似乎不涉及proTRH基因表达降低,而可能包括对垂体mRNA翻译的影响。我们的数据进一步支持了以下假说:尽管急性饥饿和长期食物减少这种作用的机制可能不同,但皮质酮分泌增加可能会降低TSH释放。